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Transformation: how do nematode sperm become activated and crawl?

机译:转化:线虫的精子如何被激活并爬行?

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摘要

Nematode sperm undergo a drastic physiological change during spermiogenesis (sperm activation). Unlike mammalian flagellated sperm, nematode sperm are amoeboid cells and their motility is driven by the dynamics of a cytoskeleton composed of major sperm protein (MSP) rather than actin found in other crawling cells. This review focuses on sperm from Caenorhabditis elegans and Ascaris suum to address the roles of external and internal factors that trigger sperm activation and power sperm motility. Nematode sperm can be activated in vitro by several factors, including Pronase and ionophores, and in vivo through the TRY-5 and SPE-8 pathways. Moreover, protease and protease inhibitors are crucial regulators of sperm maturation. MSP-based sperm motility involves a coupled process of protrusion and retraction, both of which have been reconstituted in vitro. Sperm motility is mediated by phosphorylation signals, as illustrated by identification of several key components (MPOP, MFPs and MPAK) in Ascaris and the characterization of GSP-3/4 in C. elegans.
机译:线虫的精子在生精过程中发生剧烈的生理变化(精子活化)。与哺乳动物的鞭毛精子不同,线虫的精子是变形虫细胞,其运动性是由主要精子蛋白(MSP)而不是在其他爬行细胞中发现的肌动蛋白组成的细胞骨架的动力学驱动的。这篇综述着重于秀丽隐杆线虫和A虫的精子,以探讨引起精子活化和精子活力的外部和内部因素的作用。线虫的精子可以通过多种因素在体外被激活,包括Pronase和离子载体,并在体内通过TRY-5和SPE-8途径被激活。此外,蛋白酶和蛋白酶抑制剂是精子成熟的关键调节剂。基于MSP的精子运动涉及突出和缩回的耦合过程,这两种过程都已在体外重建。精子活力由磷酸化信号介导,如as虫中几个关键成分(MPOP,MFP和MPAK)的鉴定以及秀丽隐杆线虫中GSP-3 / 4的鉴定所说明。

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